ライフサイエンスコーパス: Populus

1 on wood development in the model angiosperm, Populus.

2 435 individuals from a natural population of Populus.

3 nkage-linkage disequilibrium (LD) mapping in Populus.

4 bium maintenance and cell differentiation in Populus.

5 to identify ARK1 binding loci genome-wide in Populus.

6 asmonic acid (JA)-induced gene regulation in Populus.

7 tative resistance to Melampsora in leaves of Populus.

8 ent polymorphisms are prevalent in the genus Populus.

9 prior to the salicoid genome duplication in Populus.

10 h sink provisioning and drought tolerance in Populus.

11 al responses to shade in the woody perennial Populus.

12 ling were induced under enriched FR light in Populus.

13 o both sink demand and plant water status in Populus.

14 es were expressed in secondary stem xylem of Populus.

15 lishment of its mutualistic association with Populus.

16 scription factor PdNF-YB21 was isolated from Populus.

17 rom new and publically available datasets in Populus.

18 ironmental selection and local adaptation in Populus.

19 these factors during the diversification of Populus, a model tree genus in the Northern Hemisphere.

20 d we consequently named it Populus tremula x Populus alba (Pta) LBD1.

21 ts) to address this topic in hybrid zones of Populus alba and P. tremula, two widespread, ecologicall

22 472 seedlings from a natural hybrid zone of Populus alba and Populus tremula for genome-wide markers

23 No thylakoid isoforms could be identified in Populus alba or in Salix babylonica.

24 o water stress, transgenic Populus tremula x Populus alba plants characterized by the strong down-reg

25 following shoot removal in Populus tremula x Populus alba softwood cuttings in the absence of exogeno

26 abidopsis (Arabidopsis thaliana) and poplar (Populus alba x grandidentata), and a series of analytica

27 Populus alba x P. glandulosa is used widely in scientifi

28 n were modified in poplar (Populus tremula x Populus alba) by specifically down-regulating CINNAMYL A

29 Poplars (Populus tremula x Populus alba) down-regulated for cinnamoyl-CoA reductase

30 activation-tagged poplar (Populus tremula x Populus alba) mutant with enhanced woody growth and chan

31 wn-regulated poplar trees (Populus tremula x Populus alba) on the bacterial rhizosphere microbiome an

32 s as well as hybrid aspen (Populus tremula x Populus alba) overexpressing the MYB134 transcription fa

33 n of CSE in hybrid poplar (Populus tremula x Populus alba) resulted in up to 25% reduced lignin depos

34 erized response of poplar (Populus tremula x Populus alba) roots to low nitrogen (LN), which involves

35 he early-flowering female poplar clone 6K10 (Populus alba) to suppress the expression of its two dupl

36 ence that, in gray poplar (Populus tremula x Populus alba), Suc enters the phloem through plasmodesma

37 Using hybrid poplar (Populus tremula x Populus alba), we applied this strategy and examined fie

38 y stands of hybrid poplar (Populus tremula x Populus alba).

39 od anatomy (Quercus robur, Populus tremula x Populus alba, and Pinus pinaster).

40 members, we searched the genome sequences of Populus and Arabidopsis, and identified, respectively, 9

41 chocarpa and 15 SSPs exhibiting expansion in Populus and closely related lineages.

42 Focusing on Eucalyptus, Pinus, Populus and Pseudotsuga - genera that represent diverse

43 In contrast, we found a single ICS gene in Populus and six other sequenced plant genomes, pointing

44 oss of conifers and large increases of Acer, Populus, and Quercus in northern hardwoods, whereas to t

45 genetic variation in narrowleaf cottonwood, Populus angustifolia, a dominant riparian tree.

46 ied a riparian broadleaf angiosperm species, Populus angustifolia, growing on water with a constant d

47 Almost all plants in the genus Populus are dioecious (i.e. trees are either male or fem

48 phenotypic variation in freeze resistance of Populus balsamifera across latitude and the growing seas

49 ion in male and female flowers and leaves of Populus balsamifera to assess the extent of sex-biased e

50 Using balsam poplar (Populus balsamifera) as a case study, we demonstrate how

51 nes for adaptive phenology in balsam poplar, Populus balsamifera, a widespread forest tree whose rang

52 of a single widely distributed tree species, Populus balsamifera, with variation represented in globa

53 vergence of host species Populus tremula and Populus balsamifera/Populus trichocarpa at 5 Ma.

54 d sulfated LCOs enhanced the colonization of Populus by L. bicolor Compared with the wild-type Populu

55 de (programs and scripts) for processing the Populus ChIP-seq data are provided within a publically a

56 rt here the functional characterization of a Populus class III HD ZIP gene, popREVOLUTA (PRE), that d

57 cloning and functional characterization of a Populus class-I KNOX homeobox gene, ARBORKNOX2 (ARK2), w

58 Sequencing of 184 RT-PCR Populus clones revealed 37 alternative splice variants,

59 Here, we investigated the function of the Populus CLV3/ESR-RELATED 47 (PttCLE47) gene during secon

60 We found that the trunks of Populus davidiana emitted large quantities of CH4 during

61 Here, the Populus deltoides (Marsh.) RanBP gene (PdRanBP) was isol

62 Cut leaves of Populus deltoides and Brassica napus were placed in eith

63 lators of the lignin biosynthesis pathway in Populus deltoides by combining genome, transcriptome, an

64 also demonstrate neutral loss scanning on a Populus deltoides leaf and on a lignin sample, both sign

65 lion expressed sequence tag (EST) reads from Populus deltoides leaf transcriptome and reconstructed f

66 To aid in the investigation of the Populus deltoides microbiome, we generated draft genome

67 and 19 other diverse bacteria isolated from Populus deltoides roots.

68 ter availability on seedlings of two native (Populus deltoides spp. monilifera, Salix exigua) and thr

69 We examined communities associated with Populus deltoides using rRNA gene sequence analyses and

70 We pollinated Populus deltoides with gamma-irradiated Populus nigra po

71 In this study, poplars (Populus deltoides x nigra) and Arabidopsis thaliana were

72 In this study, poplar trees (Populus deltoides x nigra) were exposed hydroponically t

73 Poplar (Populus deltoides x nigra, DN34) was used to investigate

74 Poplars (Populus deltoides x nigra, DN34) were exposed to PCB3 wi

75 Poplars (Populus deltoides x nigra, DN34), a model plant with com

76 rifera) to the north vs. eastern cottonwood (Populus deltoides) and sweet gum (Liquidambar styraciflu

77 emission in oak (Quercus robur) and poplar (Populus deltoides) leaves in order to understand the reg

78 Here, we conducted the first GWAS in Populus deltoides, a genetically diverse keystone forest

79 st in Salix exigua, moderately supported for Populus deltoides, and indiscernible in Salix amygdaloid

80 s a plant-associated bacterium isolated from Populus deltoides, and its draft genome sequence is repo

81 ago truncatula, dicot, Leguminosae), poplar (Populus deltoides, dicot, Salicaceae), and switchgrass (

82 Here, we pair work in poplar (Populus) describing one of the smallest sex-determining

83 Foliar endophytes of Populus do not induce the hypersensitive response associ

84 Populus euphratica has been deemed to be a promising can

85 Populus euphratica Olivier, which has been considered as

86 a mapping experiment using Euphrates poplar (Populus euphratica), a so-called hero tree able to grow

87 x1) and GA-insensitive (35S:rgl1) transgenic Populus exhibited increased lateral root proliferation a

88 Transgenic Populus expressing a microRNA-resistant form of PRE pres

89 formed ecological niche models (gENMs) using Populus fremontii (Salicaceae), a widespread tree specie

90 common garden with two native tree species, Populus fremontii and P. angustifolia, and their natural

91 old change cutoff = 0) from 36,007 expressed Populus gene models.

92 Here, we identified a Populus gene, PsnSHN2, a counterpart of the Arabidopsis

93 idate sORF genes, 56 were new to the current Populus genome annotation.

94 ribution to the continued improvement of the Populus genome assembly, while demonstrating the feasibi

95 ere we performed a comprehensive scan of the Populus genome for dosage-sensitive loci affecting quant

96 hIP-seq data have been integrated within the Populus Genome Integrative Explorer (PopGenIE) where the

97 istics, and evolution of ARK1 binding in the Populus genome.

98 Thus, the chromosomal synteny in Populus has been remarkably maintained after nearly 14 m

99 belonging to five different sections within Populus, have maintained a remarkably conserved karyotyp

100 nd associated putative target genes for four Populus homeodomain transcription factors expressed duri

101 Populus hopeiensis exhibits exceptional tolerance to wat

102 When expressed in Arabidopsis, Populus ICS again underwent alternative splicing, but di

103 The splice-site sequences of Populus ICS are unusual, suggesting a causal link betwee

104 Populus ICS primarily functions in phylloquinone biosynt

105 Populus ICS underwent extensive alternative splicing tha

106 utes to the dimensions of vessel elements in Populus, impacting hydraulic conductivity.

107 ed LCOs enhanced lateral root development in Populus in a calcium/calmodulin-dependent protein kinase

108 portantly, calcium spiking in the host plant Populus in a CASTOR/POLLUX-dependent manner.

109 The SA response in Populus involved a reprogramming of carbon uptake and pa

110 othesize that duplicate gene preservation in Populus is driven by a combination of subfunctionalizati

111 ts) of potential QTLs for growth traits in a Populus linkage population (1200 progeny) and a natural

112 In Populus, low nitrogen (LN) elicits rapid and vigorous la

113 In poplar (genus Populus), MYB134 is known to regulate proanthocyanidin b

114 urements of isoprene emission from leaves of Populus nigra and hybrid aspen (Populus tremula x P. tre

115 introduced into the commercial hybrid poplar Populus nigra L. x P. maximowiczii A.

116 ated Populus deltoides with gamma-irradiated Populus nigra pollen to produce >500 F1 seedlings contai

117 ranched and branched hybrid poplar saplings (Populus nigra x P. deltoides).

118 Black poplar (Populus nigra) is a potential feedstock for cellulosic e

119 e in trees constitutively emitting isoprene (Populus nigra) or monoterpenes (Quercus ilex), or that d

120 a nonfunctional SOT1 allele in black poplar (Populus nigra) was shown to correlate with the absence o

121 al activity of flavan-3-ols in black poplar (Populus nigra), which include both monomers, such as cat

122 However, all members of the expanded Populus nucleoredoxin-1 family exhibited increased expre

123 All 26 Populus OMT genes were located in segmental duplication

124 ates functional diversity and overlap of the Populus PHYB1 and PHYB2 in regulating shade responses.

125 Populus PHYB1 rescued Arabidopsis phyB mutant phenotypes

126 n initial attempt at deciphering the role of Populus PHYs by evaluating transcriptional reprogramming

127 e expression and subcellular localization of Populus PHYs was studied by quantitative real-time PCR (

128 Trees in the genus Populus (poplar) contain phenolic secondary metabolites

129 ence in Populus trichocarpa Nisqually-1, the Populus reference genome, growing in its natural habitat

130 In several other species, including Populus, SA is derived primarily from the phenylpropanoi

131 Expression profiling of OMT genes in Populus showed that only PoptrOMT25 was differentially e

132 d salirepin-7-sulfate in a subset of poplar (Populus sp.) and willow (Salix sp.) species revealed a b

133 corn stover, sugar cane bagasse, and poplar (Populus sp.).

134 dimorphism using >1300 individuals from two Populus species and assessing 96 non-reproductive functi

135 interspecific hybrid family derived from two Populus species during the first 24 yr of ontogeny.

136 We demonstrate that five Populus species, belonging to five different sections wi

137 In several tree species, including Populus species, the majority of this carbon is derived

138 e and improve saccharification efficiency in Populus species.

139 s Tricholoma populinum is host-specific with Populus species.

140 atural hybrids of two ecologically divergent Populus species.

141 The Populus-specific genes are candidates for carbon sequest

142 Elite poplar (Populus spp) varieties are created through interspecific

143 one of the most abundant proteins in poplar (Populus spp) xylem, but its biological role has remained

144 Field study of transgenic poplars (Populus spp.) for over 6 years showed that downregulatio

145 Poplar (Populus spp.) is a tree species considered for the remed

146 al properties of some representative poplar (Populus spp.) isoforms were investigated.

147 are highly susceptible to competition (e.g. Populus spp.) or to biotic disturbances (e.g. Abies bals

148 Isoprene emissions from poplar (Populus spp.) plantations can influence atmospheric chem

149 Specifically, in poplar (Populus spp.), the formation of xylem embolisms leads to

150 naling, and response are affected in poplar (Populus spp.)-Laccaria bicolor ECM roots.

151 productive growth in woody perennial poplar (Populus spp.).

152 In Populus spp., it has long been thought that one monolign

153 The Populus sucrose (Suc) transporter 4 (PtaSUT4), like its

154 sed network connectivity in SA-overproducing Populus, suggesting a previously undescribed role in SA-

155 In source leaves of Populus, SUT4 is the predominantly expressed gene family

156 framework was confirmed by simulation and a Populus szechuanica var.

157 framework was confirmed by simulation and a Populus szechuanica var. tibetica data set.

158 We constructed phylogenetic trees of 29 Populus taxa using 80 individuals based on re-sequenced

159 will reduce growth more for native Salix and Populus than for drought-tolerant exotic species.

160 sticated populations may be more feasible in Populus than previously assumed.

161 on of clonally propagated F1 hybrid lines of Populus that saturate the genome 10-fold with deletions

162 us by L. bicolor Compared with the wild-type Populus, the colonization of CASTOR/POLLUX and CCaMK RNA

163 s were compared among Arabidopsis, Oryza and Populus to identify differential gene (DG) sets that are

164 ein-coding genes suggests that assignment of Populus to Malvidae, rather than Fabidae, is warranted.

165 ybrid population of the model hardwood plant Populus to uncover transcriptional networks in xylem, le

166 n 435 individuals of a natural population of Populus tomentosa.

167 Phenotypes of Populus transgenic lines and the expression of candidate

168 Here, we show, in Populus trees, that initial gravity perception and respo

169 e processes in a trispecific hybrid swarm of Populus trees.

170 ter the estimated divergence of host species Populus tremula and Populus balsamifera/Populus trichoca

171 om a natural hybrid zone of Populus alba and Populus tremula for genome-wide markers from reduced rep

172 ascular cambium, and wood-forming tissues of Populus tremula The transcriptome comprised 28,294 expre

173 Transgenic Populus tremula x alba (717-1B4) plants with reduced exp

174 re of the mature leaves of the model species Populus tremula x alba across all seven hierarchical ord

175 We report that transgenic Populus tremula x alba expressing a bacterial SA synthas

176 show that CRISPR-knockout of 4CL1 in poplar (Populus tremula x alba) preferentially reduced syringyl

177 tor of VPC, to modulate the timing of VPC in Populus tremula x alba, Zea mays, and Arabidopsis thalia

178 om leaves of Populus nigra and hybrid aspen (Populus tremula x P. tremuloides) in response to changes

179 opsis thaliana, and we consequently named it Populus tremula x Populus alba (Pta) LBD1.

180 poplar response to water stress, transgenic Populus tremula x Populus alba plants characterized by t

181 eling during 48 h following shoot removal in Populus tremula x Populus alba softwood cuttings in the

182 ent and composition were modified in poplar (Populus tremula x Populus alba) by specifically down-reg

183 Poplars (Populus tremula x Populus alba) down-regulated for cinna

184 y characterized an activation-tagged poplar (Populus tremula x Populus alba) mutant with enhanced woo

185 ield-grown, CCR-down-regulated poplar trees (Populus tremula x Populus alba) on the bacterial rhizosp

186 of catechin and PAs as well as hybrid aspen (Populus tremula x Populus alba) overexpressing the MYB13

187 hat down-regulation of CSE in hybrid poplar (Populus tremula x Populus alba) resulted in up to 25% re

188 sly poorly characterized response of poplar (Populus tremula x Populus alba) roots to low nitrogen (L

189 experimental evidence that, in gray poplar (Populus tremula x Populus alba), Suc enters the phloem t

190 Using hybrid poplar (Populus tremula x Populus alba), we applied this strateg

191 ar-old high-density stands of hybrid poplar (Populus tremula x Populus alba).

192 ith contrasting wood anatomy (Quercus robur, Populus tremula x Populus alba, and Pinus pinaster).

193 t evolved with Populus trichocarpa (Ptr) and Populus tremula x Populus tremuloides (Ptt) were studied

194 SVT regeneration system in the hybrid aspen (Populus tremula x Populus tremuloides) clone T89 to bypa

195 The transgenic hybrid aspens (Populus tremula x Populus tremuloides) overexpressing ea

196 in the strong isoprene emitter hybrid aspen (Populus tremula x Populus tremuloides), and used rapid c

197 ension wood and normal wood of hybrid aspen (Populus tremula x Populus tremuloides).

198 nhibition in isoprene-emitting hybrid aspen (Populus tremula x Populus tremuloides).

199 condary cell wall formation in hybrid aspen (Populus tremula x Populus tremuloides).

200 in the strong isoprene emitter hybrid aspen (Populus tremula x Populus tremuloides).

201 rification, and functional reconstitution of Populus tremula x tremuloides CesA8 (PttCesA8), implicat

202 ambial development, we engineered transgenic Populus tremula x tremuloides trees with an elevated cyt

203 PECTIN METHYLESTERASE1 (PtxtPME1) in aspen (Populus tremula x tremuloides) triggers the formation of

204 y growth and wood formation in hybrid aspen (Populus tremula x tremuloides) using an RNA interference

205 poration to developing wood of hybrid aspen (Populus tremula x tremuloides).

206 the most abundantly expressed SUT isoform in Populus tremulaxalba, PtaSUT4, is a tonoplast (Group IV)

207 ase in the thermotolerance of hybrid poplar (Populus tremulaxPopulus alba) through overexpression of

208 (FTIRI) was developed that entailed growing Populus tremulodes seedlings on a thin, nutrient-enriche

209 ulus trichocarpa (Ptr) and Populus tremula x Populus tremuloides (Ptt) were studied from their ecolog

210 The scheme was upscaled to Populus tremuloides forests across Colorado, USA, using

211 ea increment series from 40 trembling aspen (Populus tremuloides Michx.) sites along a latitudinal gr

212 -width chronologies from 40 trembling aspen (Populus tremuloides Michx.) sites along a latitudinal gr

213 ent widespread mortality of trembling aspen (Populus tremuloides Michx.).

214 Arabidopsis (Arabidopsis thaliana) CAD5 and Populus tremuloides sinapyl alcohol dehydrogenase, respe

215 High concentrations of leaf tannins in Populus tremuloides were correlated with (15) N recovery

216 iyear widespread die-off of trembling aspen (Populus tremuloides) across much of western North Americ

217 (Malacosoma disstria) and host trees aspen (Populus tremuloides) and birch (Betula papyrifera).

218 ies of four target species: trembling aspen (Populus tremuloides) and paper birch (Betula papyrifera)

219 od xylem in comparison with trembling aspen (Populus tremuloides) and white spruce (Picea glauca).

220 ystem in the hybrid aspen (Populus tremula x Populus tremuloides) clone T89 to bypass the limitation

221 espread and climate-induced trembling aspen (Populus tremuloides) forest mortality in western North A

222 transgenic hybrid aspens (Populus tremula x Populus tremuloides) overexpressing each selected TF gen

223 e carbon stress in isolated trembling aspen (Populus tremuloides) ramets.

224 ponderosa) and angiosperm (trembling aspen - Populus tremuloides) tree species in the southwestern US

225 rene emitter hybrid aspen (Populus tremula x Populus tremuloides), and used rapid changes in ambient

226 rmal wood of hybrid aspen (Populus tremula x Populus tremuloides).

227 ene-emitting hybrid aspen (Populus tremula x Populus tremuloides).

228 formation in hybrid aspen (Populus tremula x Populus tremuloides).

229 rene emitter hybrid aspen (Populus tremula x Populus tremuloides).

230 uding Pinus strobus, Platycladus orientalis, Populus tremuloides, Thuja koraiensis, Thuja occidentali

231 two altitudinal transects in the model tree Populus trichocapra.

232 of the known miRNAs from various tissues of Populus trichocarpa (black cottonwood).

233 Using hydroponically grown Populus trichocarpa (clone Nisqually-1), we have establi

234 Two nectary types that evolved with Populus trichocarpa (Ptr) and Populus tremula x Populus

235 We resequenced 16 genomes of the model tree Populus trichocarpa and genotyped 120 trees from 10 subp

236 eudo-backcross progeny of 154 individuals of Populus trichocarpa and P. deltoides analyzed with long-

237 cies Populus tremula and Populus balsamifera/Populus trichocarpa at 5 Ma.

238 By functionally screening a subset of Populus trichocarpa BAHD/HXXXD acyltransferases, we iden

239 nscript and protein abundances in transgenic Populus trichocarpa based on targeted knockdowns of spec

240 We identified and studied Populus trichocarpa genes, PtrHAB1 through PtrHAB15, bel

241 bundance and distribution of foliar fungi of Populus trichocarpa in wild populations across its nativ

242 e changes during seasonal leaf senescence in Populus trichocarpa Nisqually-1, the Populus reference g

243 lymorphism (SNP)-phenotype associations in a Populus trichocarpa population distributed from Californ

244 Using RNA sequencing of Populus trichocarpa roots in mutualistic symbiosis with

245 procedure for isolation and transfection of Populus trichocarpa stem differentiating xylem protoplas

246 ns peak in the developing phloem tissue of a Populus trichocarpa stem.

247 ence genome from the oldest branch of a wild Populus trichocarpa tree with two dominant stems which h

248 ection scans and association analyses of 544 Populus trichocarpa trees to reveal genomic bases of ada

249 representing 1,100 individual undomesticated Populus trichocarpa trees, 47 extreme phenotypes were se

250 parenchyma cells after embolism formation in Populus trichocarpa trees.

251 sence of quantitative trait loci (QTLs) in a Populus trichocarpa x P. deltoides F(2) population.

252 studies of approximately 400 natural poplar (Populus trichocarpa) accessions phenotyped for 60 ecolog

253 ation experiment using the black cottonwood (Populus trichocarpa) foliar microbiome, we manipulated h

254 this study, we show that transgenic poplar (Populus trichocarpa) lines can be solubilized without an

255 ory, the tree species western balsam poplar (Populus trichocarpa) produces a variety of Phe-derived m

256 tuberosum), Medicago truncatula, and poplar (Populus trichocarpa) revealed conserved ratios of the AS

257 rect evidence demonstrating that the poplar (Populus trichocarpa) wood-associated NAC domain transcri

258 on a screen of natural accessions of poplar (Populus trichocarpa), revealing that the leaf cuticular

259 er 40% had up-regulated orthologs in poplar (Populus trichocarpa), rice (Oryza sativa), or Chlamydomo

260 unction endoglucanase from black cottonwood (Populus trichocarpa), which reveals a small, newly recog

261 nd salirepin-7-sulfate, in black cottonwood (Populus trichocarpa).

262 aldoxime formation in western balsam poplar (Populus trichocarpa).

263 spruce, grape (Vitis vinifera), and poplar (Populus trichocarpa).

264 abidopsis (Arabidopsis thaliana) and poplar (Populus trichocarpa).

265 ous root formation in the model tree poplar (Populus trichocarpa).

266 acetylesterase (PAE1) from black cottonwood (Populus trichocarpa).

267 ally expressed in developing wood of poplar (Populus trichocarpa).

268 ange within populations of black cottonwood (Populus trichocarpa).

269 omosome, was applied to the chromosome 19 of Populus trichocarpa, an incipient sex chromosome, deciph

270 sphate synthase (DXS) enzyme was cloned from Populus trichocarpa, and the recombinant protein (PtDXS)

271 eductase (CCR) families in wood formation in Populus trichocarpa, including the regulatory effects of

272 nstructed a genome-scale metabolic model for Populus trichocarpa, the first for a perennial woody tre

273 In stem differentiating xylem (SDX) of Populus trichocarpa, two cinnamic acid 4-hydroxylases (P

274 ) biosynthesis during stem wood formation in Populus trichocarpa, two enzymes, Ptr4CL3 and Ptr4CL5, c

275 two reference plant species, A. thaliana and Populus trichocarpa, with annotations based on UniProt,

276 ion of D14 homologs in the model woody plant Populus trichocarpa.

277 evealed homology with a predicted protein of Populus trichocarpa.

278 iating xylem (SDX), in the model woody plant Populus trichocarpa.

279 wood-forming tissue of the model woody plant Populus trichocarpa.

280 two monolignol 4CLs, Ptr4CL3 and Ptr4CL5, in Populus trichocarpa.

281 ive of SND1 transcriptional network genes in Populus trichocarpa.

282 ly duplicated genes in the model forest tree Populus trichocarpa.

283 arCyc, from the recently sequenced genome of Populus trichocarpa.

284 he reference genome of the model woody plant Populus trichocarpa.

285 ly contrasting populations of the model tree Populus trichocarpa.

286 is thaliana, papaya [Carica papaya], poplar [Populus trichocarpa], and grape [Vitis vinifera]), we de

287 pressing a constitutively active form of the Populus type-B cytokinin response regulator PtRR13 (Delt

288 or goal for bioenergy crops, such as poplar (Populus), which will be grown on marginal lands with lit

289 ination regions of the closely related genus Populus, which is located on a different chromosome.

290 lower than expected from previous studies in Populus, with r(2) dropping below 0.2 within 3-6 kb.

291 The MALDI-LIT-MS images of young Populus wood stem showed even distribution of both cellu

292 and non-isoprene-emitting (NE) gray poplar (Populus x canescens) after acute ozone fumigation.

293 Knockdown lines of CYP79D6/7 in gray poplar (Populus x canescens) exhibited a decreased emission of a

294 r pressure deficit (VPD) in two gray poplar (Populus x canescens) lines: wild type and abscisic acid-

295 ated-downregulation of AADC1 in gray poplar (Populus x canescens) resulted in decreased accumulation

296 e-mediated knockdown of SOT1 in gray poplar (Populus x canescens) resulted in decreased levels of sul

297 Rays from wood samples of poplar (Populus x canescens) were enriched by laser microdissect

298 In this study, poplar plants (Populus x canescens) were exposed to water stress to inv

299 es and physiological performance in poplars (Populus x canescens) with either wild-type or RNAi-suppr

300 g (IE) and nonisoprene-emitting (NE) poplar (Populus x canescens).